rs730880754

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs730880754(A;A)

Make rs730880754(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424131

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880754
dbSNP (classic)	rs730880754
ClinGen	rs730880754
ebi	rs730880754
HLI	rs730880754
Exac	rs730880754
Gnomad	rs730880754
Varsome	rs730880754
LitVar	rs730880754
Map	rs730880754
PheGenI	rs730880754
Biobank	rs730880754
1000 genomes	rs730880754
hgdp	rs730880754
ensembl	rs730880754
geneview	rs730880754
scholar	rs730880754
google	rs730880754
pharmgkb	rs730880754
gwascentral	rs730880754
openSNP	rs730880754
23andMe	rs730880754
SNPshot	rs730880754
SNPdbe	rs730880754
MSV3d	rs730880754
GWAS Ctlg	rs730880754

Max Magnitude

0

ClinVar
Risk	rs730880754(A;A)
Alt	rs730880754(A;A)
Reference	Rs730880754(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23893340C>T
CLNSRC
CLNACC	RCV000158562.2,